Evaluating lignin degradation under limited oxygen conditions by bacterial isolates from forest soil

Lignin, a heterogeneous aromatic polymer present in plant biomass, is intertwined with cellulose and hemicellulose fibrils, posing challenges to its effective utilization due to its phenolic nature and recalcitrance to degradation. In this study, three lignin utilizing bacteria, Klebsiella sp. LEA1, Pseudomonas sp. LEA2, and Burkholderia sp. LEA3, were isolated from deciduous forest soil samples in Nan province, Thailand. These isolates were capable of growing on alkali lignin and various lignin-associated monomers at 40 °C under microaerobic conditions. The presence of Cu2+ significantly enhanced guaiacol oxidation in Klebsiella sp. LEA1 and Pseudomonas sp. LEA2. Lignin-related monomers and intermediates such as 2,6-dimethoxyphenol, 4-vinyl guaiacol, 4-hydroxybenzoic acid, benzoic acid, catechol, and succinic acid were detected mostly during the late stage of incubation of Klebsiella sp. LEA1 and Pseudomonas sp. LEA2 in lignin minimal salt media via GC–MS analysis. The intermediates identified from Klebsiella sp. LEA1 degradation suggested that conversion and utilization occurred through the β-ketoadipate (ortho-cleavage) pathway under limited oxygen conditions. The ability of these bacteria to thrive on alkaline lignin and produce various lignin-related intermediates under limited oxygen conditions suggests their potential utility in oxygen-limited processes and the production of renewable chemicals from plant biomass.


Bacteria isolation and identification
A total of 16 bacterial colonies with different colony sizes and morphologies were selected from the lignin enrichment process.The selected bacterial isolates were those that exhibited utilization or tolerance to the presence of phenolic compounds prevalent in lignin under limited oxygen conditions.For initial screening, colonies that grew on L-MSM (Lignin minimal salt media) with alkali lignin as the sole carbon source were selected for further screening.Afterward, the selected colonies were streaked onto carboxymethyl cellulose (CMC) agar plates to further select colonies with the ability to utilize cellulose as an energy source in addition to lignin.Nine bacterial isolates were identified by 16S rDNA sequencing to be closely related to Klebsiella sp., four were closely related to Burkholderia sp., and three to Pseudomonas sp., (Supplementary Table S1).The reported growth of the bacteria is consistent with the previous evidence in that all three genera possess lignin degrading ability 33,34 .Selected representative isolates, Klebsiella sp.LEA1, Pseudomonas sp.LEA2 and Burkholderia sp.LEA3 (16S rDNA sequences are available in the NCBI database with accession numbers MW186661, MW193077, and MW193078, respectively) were chosen for further characterization.The phylogenetic trees of each isolate were constructed along with the bacteria in the same genus retrieved from the NCBI database.According to the phylogenetic trees, Klebsiella sp.LEA1 is the most closely related to Klebsiella sp.FX0042 isolated from the soil in China.The bacterium is also grouped into the same clade with Klebsiella sp.P5 and K. variicola JM13 (Fig. 1A).For Pseudomonas sp.LEA2 and Burkholderia sp.LEA3, the taxonomic analysis revealed the closest relationship of the bacteria to P. aeruginosa PA0504 and B. vietnamiensis la1a4, respectively (Fig. 1B,C).

Growth on lignin monomers and effect of copper (Cu 2+ ) on guaiacol oxidation
In preliminary experiments, Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 were able to grow on minimal salts media agar plates containing three types of model lignin monomers (guaiacol, veratryl alcohol, and 2,6-Dimethylphenol (2,6 DMP)) [35][36][37] as the sole carbon source, while the growth of Burkholderia sp.LEA3 was only observed on veratryl alcohol and 2,6 DMP.No growth observation was found for Burkholderia sp.LEA3 on MSM supplemented with guaiacol (Supplementary Table S2).For nutritionally rich medium, the isolates could grow on LB media supplemented with guaiacol except for Burkholderia sp.LEA3, which exhibited no growth.Copper (Cu 2+ ) has been reported to be present at the active site of laccase enzyme 38 , therefore, improvement of lignindegrading ability with the addition of Cu 2+ was determined.Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 showed enhanced guaiacol oxidation with the presence of Cu 2+ in the guaiacol medium (Fig. 2A).Oxidation was greatly increased when the bacteria were grown on LB based medium.Guaiacol is a major aromatic monomer found in depolymerized lignin; therefore, Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 were selected for further analyses based on the oxidation activity.

Growth characteristic and alkaline lignin utilization of the isolates
Growth of Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 in alkali lignin containing L-MSM was observed over a period of 7 days (Fig. 2B).Although Pseudomonas sp.LEA2 and Klebsiella sp.LEA1 were initially inoculated at an equivalent OD 600 of 0.1 with slightly different inoculum (9.20 ± 0.85 × 10 7 and 4.52 ± 0.35 × 10 7 CFU/ mL, respectively), Pseudomonas sp.LEA2 exhibited an accelerated growth rate in the first 3 days compared to Klebsiella sp.LEA1.Both isolates exhibited steady growth and reached their maximum cell density at day 3 of www.nature.com/scientificreports/ the total phenolic compound was monitored through the reduction in absorbance at 280 nm (Fig. 2C).Both isolates exhibited a pronounced decrease in detected absorbance, indicating a reduction in total phenolic content.
Given the potential influence of various molecules and lignin internalization by the bacteria on A280, additional experiments were subsequently conducted to conclusively support lignin-degrading ability.
The surface morphology of the lignin samples was also investigated using a scanning electron microscope (SEM) to assess the potential lignin-degrading ability of the bacteria.SEM images revealed that while control samples appeared relatively intact; samples treated with Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 exhibited rough and porous surfaces after 7 days of incubation under aerobic and oxygen limited conditions (Fig. 3), suggesting potential lignin degradation.Gel permeation chromatography (GPC) was further employed to demonstrate the potential lignin-depolymerizing ability of the bacteria.Samples of alkali lignin after a 7-day incubation with Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 in L-MSM under microaerobic conditions were extracted, and the results are summarized in Table 1.Changes in molecular weight distribution were supported by a reduction in number average molecular weight (Mn) from 791.7 ± 7.5 in the control sample to 714.0 ± 9.2 in Klebsiella sp.LEA1 and 734.3 ± 24.8 in Pseudomonas sp.LEA2.The control alkaline lignin displayed a weight average molecular weight (Mw) of 1353.7 ± 3.1 Da over a 7-day incubation period.In contrast, the samples treated with Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 exhibited a significant decrease in the Mw of alkaline lignin, reaching 1107.3 ± 20.2 Da and 1142.7 ± 44.6 Da, respectively (Fig. 4A).The shift of the peak towards the higher retention time side also demonstrated potential depolymerization of alkaline lignin by the bacterial isolates (Fig. 4B).A decrease in the polydispersity index indicates a limited molecular weight distribution of the alkaline lignin, potentially resulting from the depolymerization of large lignin molecules.Considering the observations of the reduction in Mw, Mn, along with peak shift, could suggest capacity of lignin degradation or utilization by the bacterial isolates.

Analysis of alkaline lignin degradation products
GC-MS analysis was performed to identify products resulting from lignin utilization by both Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 at days 3 and 7 of incubation (Table 2, Supplementary Fig. 3).Similar intermediates and products such as 4-vinyl guaiacol, isovanillyl alcohol, and 3-vanillyl propanol were detected in both isolates.Additionally, compounds such as phenol, 3,5-dimethyl cyclopentenolone, vanilonitrile, 2,6-dimethoxyphenol, vanillyl alcohol, eicosanoic acid were exclusively detected in Pseudomonas sp.LEA2, while several unique compounds such as pentanoic acid, cinnamic acid, and 4-hydroxybenzoic acid were only observed in Klebsiella sp.www.nature.com/scientificreports/LEA1.Differences in lignin-derived intermediates and products between the two isolates suggest the employment of different pathways in lignin degradation.On day 7 of incubation under microaerobic conditions, certain organic acids such as butanoic acid, benzoic acid, and benzenepropanoic acid, which were absent on day 0 or 3 of incubation, were detected in the control samples.Although this indicates some degree of abiotic degradation in the control samples, a clear distinction was observed among the detected compounds in samples of Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 compared to the control at day 7, supporting the presence of biotic degradation in the samples (Table 2).Despite an array of intermediates and products detected in both samples on day 7, none of the isovaleric acid, butanoic acid, benzenepropanoic acid or vanillin (present in control samples) were found in the samples inoculated with either of the two bacterial isolates, suggesting the utilization of the lignin-related compounds by the bacteria.Furthermore, the presence of benzoic acid, cinnamic acid, and catechol hinted at the use of the catechol branch of the β-ketoadipate pathway (ortho-cleavage) in Klebsiella sp.LEA1 under oxygen limited conditions (Fig. 5).Different lignin intermediates were identified in samples inoculated with Pseudomonas sp.LEA2 by GC-MS analysis as mentioned earlier (Table 2).However, no obvious indicator compounds or intermediates provides guidance for the pathway likely utilized by the isolate.
The dependence of lignin-degrading enzymes on oxygen has been previously reported 39 .Therefore, degradation products of lignin in Klebsiella sp.LEA1 were also investigated under aerobic conditions.In contrast to the microaerobic condition, most phenolic aromatics or lignin monomers such as benzeneacetic acid, vanillin, homovanillyl alcohol, and 4-vinyl guaiacol present in the control samples were not detected in the inoculated samples by day 3 of incubation (Table S3).By day 7, guaiacol and coniferyl alcohol were absent in the sample.Interestingly, while some lignin-related compounds were no longer detected in the sample at day 7, vanillic acid was retained throughout the incubation period (Table S3).This suggests that guaiacol degradation was greatly improved under aerobic conditions.

Discussion
Lignin-degrading bacteria such as Enterobacter ligninolyticus, Burkholderia sp.H1, Bacillus pumilus, and Bacillus atrophaeus have previously been reported from soil samples 6,26,27,31 .Most lignin-degrading bacteria belong to three major classes: Actinomycetes, α-Proteobacteria, and γ-Proteobacteria 33 .Tropical forest soils have a rich microbial diversity and active lignocellulolytic microorganisms responsible for a high rate of plant litter decomposition compared to other biomes 31,32,40 .The genera of isolates obtained in this study (Klebsiella, Burkholderia, and Pseudomonas) showed consistency with the previous report of lignin-converting bacteria 33 .Alkali lignin and other model lignin compounds have generally been used to specifically isolate ligninolytic bacteria.Studies have also shown that microorganisms isolated on alkali lignin are able to degrade lignin present in plant biomass even though technical lignin varies in structure compared to native lignin 5,38 .The presence of these isolates in samples from different parts of Nan forest indicates their active or major involvement in lignin degradation in the environment.The ability of the isolates to grow on lignin-containing medium indicated depolymerization and their utilization of degraded compounds derived from alkaline lignin.Due to the phenolic nature of lignin, which exerts toxicity on most microorganisms by damaging cell membranes, enzymes, and nucleic acids, the ability to grow on lignin-containing media could also indicate the bacteria's capability to tolerate lignin 41 .Isolates used in this study have the potential to utilize cellulose as an additional energy source based on their ability to grow on CMC plates.This is a valuable potential for lignocellulose-degrading bacteria as lignin and cellulose are major constituents of lignocellulosic biomass.
Based on the phylogenetic tree of 16S rDNA, Klebsiella sp.LEA1 shares a high sequence similarity with the soil bacterium Klebsiella sp.strain FX0042 and Klebsiella sp.strain P5 isolated from China.The isolate was also found to be closely related to the species-annotated K. variicola strain JM13 from plant rhizosphere.For Pseudomonas sp.LEA2, our bacterium shares the same node with soil isolated P. aeruginosa strain PA0504 from China.Likewise, Burkholderia sp.LEA3 is grouped with B. vietnamiensis strain la1a4 isolated from rice in Peru.
The taxonomy result provides relevance to the bacteria and type of habitat, which could be further linked to the biological function.
The ability of Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 to grow on guaiacol, veratryl alcohol, and 2, 6-dimethoxyphenol (2,6-DMP) (Supplementary Table S2) suggests the presence of genes, pathways, or metabolisms that allow for oxidation of both phenolic and non-phenolic lignin monomers.The inability of Burkholderia sp.LEA3 to grow on guaiacol-supplemented media might be due to the toxicity of guaiacol 42,43 .Guaiacol is a predominant aromatic monomer found in depolymerized lignin 44 .It makes up parts of all lignin, especially softwood lignin 44,45 .Chow, et al. 41 reported the incapability of Streptomyces sp.D7 to further degrade guaiacol after converting vanillic acid to guaiacol via decarboxylation.Enhancement of the oxidation of guaiacol by Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 was observed when copper (100 μg/mL CuSO 4 ) was supplied in the medium (Fig. 2A).
Copper has been shown to effectively enhance the production of ligninolytic enzymes.Furthermore, numerous bacterial multi-copper oxidases or laccases have been evaluated for their ability to act on both phenolic and non-phenolic compounds 38,[46][47][48][49][50] .Therefore, it is plausible that Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 may harbor copper-binding enzymes responsible for lignin utilization.Rezaei et al. 47 reported a 13.7-fold increase in laccase production with the addition of 0.5 mM CuSO 4 compared to the basal medium in Aquisalibacillus elongatus.Aside from its role in enzyme production, the supply of Cu 2+ as an essential metal ion is pivotal for maintaining enzyme activity and overall lignin degradation efficiency.Copper serves as a cofactor in the active sites of laccases, facilitating the oxidation of lignin substrates 51 .Therefore, ensuring an adequate supply of copper ions in the growth medium is essential for maximizing the activity of ligninolytic enzymes and promoting efficient lignin degradation by bacteria.
The decline in aromatic absorbance at 280 nm indicated the reduction of the total aromatic components that occurred in the presence of Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 during the 7-day incubation period.The higher growth rate and cell density of Pseudomonas sp.LEA2 may indicate its greater tolerance to lignin or better capability of lignin depolymerization and conversion.The decline in cell growth observed after day 3 of incubation is possibly due to the accumulation of phenolic compounds and other products that can produce inhibitory effects on cell growth 52 .SEM images revealed rough surfaces and pores on the surface of lignin particles treated with isolates further indicating the potential lignin degrading ability of the isolates.Similar results have been reported in other studies that treated alkali lignin with lignin degrading bacteria 6,53 .During the process of the SEM sample preparation, the supernatant from control samples appeared colourless while the supernatant from bacteria treated samples was brownish.This phenomenon likely arises from the erosion of the lignin surface, leading to the detachment of smaller particles that are subsequently absorbed or extracted into ethanol.A similar observation was also noticed in the ethyl acetate extracts of control and bacteria treated samples for GC-MS analysis.Extracts of uninoculated samples were colourless while those of samples treated with bacteria were yellowish in colour (Supplementary Fig. 4).GPC analysis suggests that Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 possess the capability to depolymerize lignin, resulting in the production of smaller lignin molecules.This is supported by the observed shift in the chromatogram peak, signifying a decrease in the Mw , along with the accumulation of small lignin-derived molecules.It should be noted that the alkaline lignin used in this study underwent sterilization through autoclaving, a process wherein moist heat and pressure could potentially impact the structure of the alkaline lignin 54,55 .Therefore, we cannot rule out the possibility that the two isolates may also utilize the molecules degraded through abiotic degradation.Future studies aimed at assessing the utilization of small phenolic compounds, such as HPLC, could enhance precision in evaluating the degradation of lignin.
Many lignin-derived intermediates and products were detected by GC-MS analysis by day 7.It appears that most degradation products were formed or accumulated at the latter stage of incubation.Orellana, et al. 56 reported that most up-regulation of ligninolytic enzymes such as laccase, peroxidases, and aryl-alcohol dehydrogenases occurred during the mid-exponential and early stationary growth phase in Enterobacter lignolyticus SCF1.Weinstein, et al. 57 also reported the degradation of β-guaiacyl ether-linked lignin dimeric compounds during the stationary growth phase of Phanerochaete chrysosporium.Lignin-related compounds detected by GC-MS throughout 7 days of incubation under microaerobic conditions suggest that Klebsiella sp.LEA1 possibly used the catechol branch of the β-ketoadipate pathway for the metabolism of aromatic compounds obtained from alkali lignin (Fig. 5).Several lignin-related monomers such as cinnamic acid, catechol, benzoic acid and 4-hydroxybenzoic acid, which can be further degraded through the gentisate or β-ketoadipate pathways were detected after 7 days of incubation [58][59][60] .The presence of succinic acid (butanedioic acid) in the degrading samples suggests mineralization by ortho-cleavage of catechol through the β-ketoadipate pathway before finally entering the tricarboxylic acid (TCA) cycle for an energy source in Klebsiella sp.LEA1 61,62 .Our proposed mechanism of Klebsiella sp.LEA1 was in accordance with the genomic analysis of Klebsiella pneumoniae AWD5 which harbors an ortho-cleavage pathway for polyaromatic hydrocarbon degradation 63 .Although the metabolic pathway employed by Pseudomonas LEA2 cannot be established in this study, it is evident that the isolate is capable of utilizing lignin-based compounds, as inferred from the GC-MS and GPC analysis.Previous studies have demonstrated the coexistence of both protocatechuate and catechol branches within the β-ketoadipate pathway in Pseudomonas aeruginosa which are selectively used depending on the compounds or intermediates the bacterium is exposed to 64,65 .
Under aerobic incubation, most lignin-related compounds present in the samples were completely degraded by day 7 suggesting that oxygen could accelerate the degradation process in Klebsiella sp.LEA1.A previous study on Phanerochaete chrysosporium revealed enhancement of lignin dimer metabolism at increased oxygen concentrations suggesting the oxidative nature of steps involved in lignin degradation 25 .Vanillic acid has been identified as one of the major aromatic metabolites obtained from different intermediates and enzymatic reactions involved in lignin degradation.Vanillic acid can also be further degraded or mineralized to simpler compounds depending on the pathway employed by the bacteria 12,13,66,67 .As seen in Table 2 and Table S3, vanillic acid was present in samples throughout the incubation period.Although the degradation steps after the accumulation of vanillic acid are unclear based on the GC-MS result, it is possible that ligninolytic bacteria funnel vanillic acid into protocatechuic acid (Fig. 5).Protocatechuic acid is further dearomatized through the β-ketoadipate pathway by protocatechuate cleavage before finally entering the TCA cycle 12,60,67 .
Previous studies in Klebsiella and Pseudomonas have reported the presence of a complete β-ketoadipate pathway through the protocatechuate and catechol routes as well as genes and enzymes involved in lignin degradation such as peroxidases, monooxygenases, and laccase 63,[68][69][70][71] .Discrepancies observed between alkali lignin degradation patterns under aerobic and limited oxygen conditions indicate the effect of environmental factors, particularly oxygen, on lignin metabolism.As seen in the results presented here, diverse degradation products were detected under microaerobic conditions compared to aerobic conditions, while vanillic acid and vanilonitrile were the only products detected under aerobic conditions.Many of the compounds discovered under oxygen limited conditions are valuable in the food, flavour and aroma industries as well as in both pharmaceutical and cosmetic sectors 12 .Thus, microaerobic conditions might be recommended to obtain a wider profile of compounds from bacterial lignin degradation.Although some studies have reported the ability of bacteria to degrade lignin, most of these studies mainly focus on lignin degradation under aerobic conditions 59,60 .Hence, bacteria that can utilize lignin under limited oxygen conditions and elevated temperature (40 °C) would be advantageous in anoxic conditions, which are more applicable in industrial settings.Further characterization of the physiological and biochemical features of these isolates, along with an understanding of related regulatory systems, may facilitate the optimization of lignin valorization for the production of various value-added compounds, particularly under oxygen-limited conditions.

16S rDNA identification of isolates
Bacterial isolates that grew on L-MSM were cultured overnight in LB medium at 40 °C, with periodic shaking at 200 rpm.Genomic DNA was extracted from overnight cultures using the phenol-chloroform extraction method.The full length of 16S rDNA was amplified using universal primers 27F and 1492R (27F 5'-AGA GTT TGA TCC TGG CTC AG-3'; 1492R 5'-GGT TAC CTT GTT ACG ACT T-3') followed by sequencing analyses.For bacterial identification, sequence homology was compared using the Basic Local Alignment Search Tool (BLAST) against the National Center for Biological Information (NCBI) database.A phylogenetic tree of 16S rDNA was constructed by the neighbor joining method, 1000 bootstrap replications using MEGA11 software.

Growth on different lignin monomers
The ligninolytic ability of selected isolates was tested using model lignin monomers (guaiacol, veratryl alcohol, and 2, 6-dimethoxyphenol (2,6-DMP)) (Sigma-Aldrich).Guaiacol and 2, 6-DMP represented phenolic substrates, while veratryl alcohol represented a non-phenolic substrate 61 .Preculture of bacterial isolate in LB with the OD 600 of 1.0 was collected after centrifuging at 5000 × g for 5 min and washed with normal saline (0.9% NaCl) three times.The bacterial suspension was then adjusted to OD 600 of 0.1 and 5 µl of the suspension was gently dropped onto MSM plates supplemented with 0.1% (v/v) guaiacol, veratryl alcohol, and 0.1% (w/v) 2, 6-DMP.The MSM plates were incubated for 7 days at 40 °C under microaerobic conditions.

Effect of copper (Cu) on lignin degradation
0.1 g/L CuSO 4 was incorporated into LB agar and MSM agar supplemented with 0.1% (v/v) guaiacol to investigate the influence of copper on guaiacol oxidation.The sample inoculated with Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 were kept at 40 °C in microaerobic conditions for 7 days.Agar plates were examined for the oxidation of guaiacol indicated by the presence of pink or brown pigments around bacterial colonies.

Growth characteristic of the isolates and total phenolic content analysis
Based on the effect of copper on guaiacol oxidation, L-MSM was modified to contain 0.1 g/L CuSO 4 .Klebsiella sp.LEA1 Pseudomonas sp.LEA2 and were inoculated into 50 mL L-MSM at an equivalent OD 600 of 0.1.Growth of the bacterial isolates in the media over time was followed at 40 °C for 7 days under microaerobic conditions.The culture suspension was sampled on days 1, 2, 3, 5, and 7 of the incubation to determine colony forming units (CFU), as the colour of alkali lignin interfered with the turbidity of the solution.
To further test for the reduction of total phenolic content, the culture supernatant was withdrawn and acidified with concentrated hydrochloric acid (HCl) to pH 2. The sample was centrifuged at 12,000 × g for 10 min and the supernatant was collected.Total phenolic content was monitored by measuring the remaining phenolic compounds at the absorbance of 280 nm using a V530 UV/Vis spectrophotometer (Jasco, Japan).

Field emission scanning electron microscope (FE-SEM)
Visual assessment of the surface morphology and structure of lignin samples was done using a field emission scanning electron microscope (FE-SEM).Two milliliters of control (no bacterium) and inoculated samples were withdrawn after 7 days and centrifuged at 12,000 × g for 10 min.The precipitates were collected and fixed in 2.5% glutaraldehyde.Precipitates were washed twice in phosphate buffer saline (PBS) pH 7 followed by sterile distilled water.The samples were dehydrated in a gradient of 25-95% ethanol and coated with a layer of Pt/Pd alloy via critical point drying and ion sputtering.Afterward, samples were imaged with FE-SEM (Hitachi SU-8010).

Gel permeation chromatography (GPC)
The molecular weight distribution of alkaline lignin was investigated using the GPC-Tetrahydrofuran (THF) system (Waters e2695, Netherlands).A total of 0.1% of alkaline lignin was incubated in a minimal salt medium with or without bacteria at 40 °C for 7 days.Alkaline lignin in the media was collected by adding 6 M HCl, centrifuged at 12,000 × g for 10 min, and dried at 60 °C.Dried lignin was acetylated using 2 mL of equal volume of acetic anhydride and pyridine.The reaction mixture was stirred for 24 h before adding 0.1 M HCl, centrifuged at 12,000 × g for 10 min, and dried at 60 °C.Dried acetylated samples were dissolved in THF and filtered through 0.2-μm nylon membrane syringe filters.Size exclusion was performed at room temperature with THF as the mobile phase (flow rate of 1 mL min -1 ) with RI, light scattering and viscometry detectors.The calibration was performed by using polystyrene standards with the Mw range between 1250 and 920,000 g mol −1 .For GPC analysis, three independent experiments were conducted.www.nature.com/scientificreports/

Gas chromatography mass spectrometry (GC-MS) analysis of lignin degradation products
Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 isolates were grown in L-MSM under microaerobic conditions for 7 days in triplicates, while the investigation under aerobic conditions was additionally done in Klebsiella sp.LEA1.Samples were collected on days 3 and 7 of incubation.Fifty millilitres of samples were centrifuged (5000 × g, 30 min) and the supernatants were acidified to pH 1-2 using 6 M HCl.After acidification, samples were centrifuged and the supernatants were harvested.Supernatants were thoroughly extracted three times with ethyl acetate and the organic layer was collected followed by dewatering over anhydrous Na 2 SO 4 in filter paper to remove moisture.The organic layer of triplicates of each treatment was pooled together, and samples were placed in a rotary evaporator at 37 °C for further moisture removal.The residues were then resuspended in 10 mL of ethyl acetate.Two milliliters of ethyl acetate suspension were derivatized after evaporation of the solvent under nitrogen gas using 70 µL N-Methyl-N-(trimethylsilyl) trifluoroacetamide with 1% trimethylchlorosilane (MSTFA) and 40 µL Methoxamine (MOX) reagent.The mixture was heated at 40 °C for 1 h with periodic shaking.One microliter of the sample was subjected to the GC-MS (Agilent Technologies USA 5977B MSD; 7890 BGC) for separation by HP-5MS UI capillary column (29.90 m × 0.25 mm × 0.25 µm).Helium was used as a carrier gas with a flow rate of 1 mL/min.The column was held at 50 °C for 5 min and increased to 300 °C (10 °C per min, hold time: 5 min).The transfer line and ion source temperatures were maintained at 200 and 250 °C.A solvent delay of 3.5 min was selected.Electron ionization mass spectra in the range of 30-550 (m/z) were recorded at an electron energy of 70 eV.The compounds were identified by comparing the retention times of standards and data in the National Institute of Standards and Technology (NIST) library.

Conclusion
In this study, bacteria capable of converting and utilizing alkaline lignin were isolated from soil samples collected from the forest in northern Thailand.Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 were able to grow on alkali lignin and lignin monomers under microaerobic conditions and elevated temperature (40 °C).SEM images revealed the erosion of the lignin surface by the isolates, consistent with the depolymerization ability suggested by GPC analysis.The profile of compounds detected using GC-MS indicated the mineralization of lignin monomers and the possible presence of lignin-degrading enzymes, genes, and pathways such as the gentisate pathway and the β-ketoadipate pathway in Klebsiella sp.LEA1.Our results also indicate increased alkaline lignin conversion during the late stage of the incubation period of bacterial isolates.Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 possess the ability to utilize alkaline lignin under the limited oxygen conditions commonly encountered in fermentation systems.Thus, the use of these lignin-utilizing bacterium can be explored further in studies related to lignin valorization and degradation under oxygen limited conditions.

Figure 1 .
Figure 1.Phylogenetic tree of 16S rDNA The tree showing the taxonomic relationship of the three isolates, (A) Klebsiella sp.LEA1, (B) Pseudomonas sp.LEA2, and (C) Burkholderia sp.LEA3 with the bacteria in the same genus.The isolates in this study are marked in bold.

Figure 2 .
Figure 2. Bacterial growth and oxidation of guaiacol (A) Guaiacol oxidation with the presence of Cu 2+ .Effects of Cu 2+ on guaiacol oxidation on minimal salt media (MSM) and LB media supplemented with 0.1% (v/v) guaiacol.Red/brown pigmentation around bacteria colonies indicates guaiacol oxidation in the media.Guaiacol oxidation experiments were carried out in triplicates (Supplementary Fig. 1).(B) Growth of Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 in L-MSM.The results of CFU/mL were calculated from triplicate samples.(C) Decrease in total phenolic content (A 280 ) in the sample treated with Klebsiella sp.LEA1 and Pseudomonas sp.LEA2.Cultures were incubated at 40 °C for 7 days under microaerobic conditions.The absorbance of 280 nm was calculated from three independent experiments.

Figure 4 .
Figure 4. Capacity of the isolates to utilize lignin.(A) Average molecular weight of alkaline lignin.(B) GPC chromatogram of alkaline lignin.Three independent experiments were conducted (Supplementary Fig. 2), which one of the replicates is shown in (B).P < 0.05*, P < 0.01**.

Figure 5 .
Figure 5. Proposed lignin degradation pathways in Klebsiella sp.LEA1.The pathway with black arrows represents the proposed ortho-cleavage of catechol through the β-ketoadipate pathway in Klebsiella sp.LEA1 under microaerobic conditions.The pathway with red arrows represents the proposed degradation pathway in Klebsiella sp.LEA1 under aerobic conditions.The pathways were developed based on metabolites detected in GC-MS in this study.Lignin related compounds and metabolites detected in the GC-MS profile are marked in boxes.

Table 1 .
Molecular weights distribution of alkaline lignin treated with the bacterial isolates.

Table 2 .
GC -MS product analysis of control and degraded samples under microaerobic conditions.Klebsiella sp.LEA1 and Pseudomonas sp.LEA2 were grown in L-MSM under microaerobic conditions at 40 °C for 7 days." + ", compound was detected; "−", compound was not detected in culture; R.T: Retention time.